ECSP099722A - PIRIDO COMPOUNDS [2, 3-D] PIRIMIDINA-7-ONA AS PI3K-ALFA INHIBITORS FOR CANCER TREATMENT - Google Patents

PIRIDO COMPOUNDS [2, 3-D] PIRIMIDINA-7-ONA AS PI3K-ALFA INHIBITORS FOR CANCER TREATMENT

Info

Publication number
ECSP099722A
ECSP099722A EC2009009722A ECSP099722A ECSP099722A EC SP099722 A ECSP099722 A EC SP099722A EC 2009009722 A EC2009009722 A EC 2009009722A EC SP099722 A ECSP099722 A EC SP099722A EC SP099722 A ECSP099722 A EC SP099722A
Authority
EC
Ecuador
Prior art keywords
compounds
pirimidina
pirido
ona
pi3k
Prior art date
Application number
EC2009009722A
Other languages
Spanish (es)
Inventor
Longcheng Wang
Chris A Buhr
Original Assignee
Exelixis Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Exelixis Inc filed Critical Exelixis Inc
Publication of ECSP099722A publication Critical patent/ECSP099722A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
    • A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
    • A61K51/025—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus inorganic Tc complexes or compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00—Radiation therapy
    • A61N5/10—X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy
    • A61N5/1001—X-ray therapy; Gamma-ray therapy; Particle-irradiation therapy using radiation sources introduced into or applied onto the body; brachytherapy
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Abstract

La invención se refiere a compuestos de la fórmula I: Iy sus sales o solvatos farmacéuticamente aceptables, así como a métodos de preparación y uso de los compuestos.The invention relates to compounds of the formula I: I and their pharmaceutically acceptable salts or solvates, as well as methods of preparation and use of the compounds.

EC2009009722A 2007-04-11 2009-11-09 PIRIDO COMPOUNDS [2, 3-D] PIRIMIDINA-7-ONA AS PI3K-ALFA INHIBITORS FOR CANCER TREATMENT ECSP099722A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US91116007P 2007-04-11 2007-04-11
PCT/US2008/004807 WO2008127712A1 (en) 2007-04-11 2008-04-11 Pyrido [2, 3-d] pyrimidin-7-one compounds as inhibitors of pi3k-alpha for the treatment of cancer

Publications (1)

Publication Number Publication Date
ECSP099722A true ECSP099722A (en) 2009-12-28

Family

ID=39642739

Family Applications (1)

Application Number Title Priority Date Filing Date
EC2009009722A ECSP099722A (en) 2007-04-11 2009-11-09 PIRIDO COMPOUNDS [2, 3-D] PIRIMIDINA-7-ONA AS PI3K-ALFA INHIBITORS FOR CANCER TREATMENT

Country Status (26)

Country Link
US (2) US20100209340A1 (en)
EP (1) EP2142544B8 (en)
JP (1) JP2010523681A (en)
KR (1) KR20090130104A (en)
CN (1) CN101711249A (en)
AU (1) AU2008239596B2 (en)
BR (1) BRPI0810175A2 (en)
CA (1) CA2683820A1 (en)
CO (1) CO6241119A2 (en)
CR (1) CR11098A (en)
DO (1) DOP2009000242A (en)
EA (1) EA018964B1 (en)
EC (1) ECSP099722A (en)
ES (1) ES2425068T3 (en)
HK (1) HK1139941A1 (en)
IL (1) IL201209A0 (en)
MA (1) MA31336B1 (en)
MX (1) MX2009010815A (en)
MY (1) MY150747A (en)
NI (1) NI200900183A (en)
NZ (1) NZ579945A (en)
SV (1) SV2009003389A (en)
TN (1) TN2009000389A1 (en)
UA (1) UA101315C2 (en)
WO (1) WO2008127712A1 (en)
ZA (1) ZA200906648B (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006065703A1 (en) * 2004-12-13 2006-06-22 Sunesis Pharmaceuticals, Inc. Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as raf kinase inhibitors
BRPI0617159B8 (en) * 2005-10-07 2021-05-25 Exelixis Inc pi3ka inhibitor pyridopyrimidinone compounds, compositions containing them, and preparation process
JP5270353B2 (en) * 2005-10-07 2013-08-21 エクセリクシス， インク． Phosphatidylinositol 3-kinase inhibitor and method of use thereof
AU2007284562B2 (en) 2006-08-16 2013-05-02 Exelixis, Inc. Using PI3K and MEK modulators in treatments of cancer
WO2008032162A1 (en) 2006-09-15 2008-03-20 Pfizer Products Inc. Pyrido (2, 3-d) pyrimidin0ne compounds and their use as pi3 inhibitors
UA100979C2 (en) 2007-04-10 2013-02-25 Экселиксис, Инк. Methods of treating cancer using pyridopyrimidinone inhibitors of pi3k alpha
EP2142543B8 (en) * 2007-04-11 2013-07-03 Exelixis, Inc. Pyrido [2, 3-d]pyrimidin-7-one compounds as inhibitors of pi3k-alpha for the treatment of cancer
PA8843901A1 (en) * 2008-09-30 2010-05-26 PI3K PYRIMIDINONE INHIBITORS (ALFA) AND m TOR
US20120040950A1 (en) * 2009-12-22 2012-02-16 Vertex Pharmaceuticals Incorporated Isoindolinone inhibitors of phosphatidylinositol 3-kinase
TW201139436A (en) 2010-02-09 2011-11-16 Exelixis Inc Methods of treating cancer using pyridopyrimidinone inhibitors of PI3K and mTOR in combination with autophagy inhibitors
WO2012037204A1 (en) 2010-09-14 2012-03-22 Exelixis, Inc. Inhibitors of pi3k-delta and methods of their use and manufacture
WO2013056067A1 (en) * 2011-10-13 2013-04-18 Exelixis, Inc. Compounds for use in the treatment of basal cell carcinoma
CN107375289A (en) 2011-11-01 2017-11-24 埃克塞利希斯股份有限公司 For treating the compound as the kinase inhibitor of phosphatidylinositols 3 of lymphoproliferative malignant tumour

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2937284A (en) * 1958-05-01 1960-05-17 Burroughs Wellcome Co 2, 4-diamino-5, 6-dialkylpyrido (2, 3-d) pyrimidines and method
IL117923A (en) * 1995-05-03 2000-06-01 Warner Lambert Co Anti-cancer pharmaceutical compositions containing polysubstituted pyrido¬2,3-d¾pyrimidine derivatives and certain such novel compounds
US7019002B2 (en) * 2001-12-11 2006-03-28 Pharmacia & Upjohn, S.P.A. Pyridopyrimidinones derivatives as telomerase inhibitors
US20080255162A1 (en) * 2004-05-04 2008-10-16 Warner-Lambert Company Llc Pyrrolyl Substituted Pyrido[2,3-D]Pyrimidin-7-Ones and Derivatives Thereof as Therapeutic Agents
CA2624965A1 (en) * 2005-10-07 2007-04-19 Exelixis, Inc. Pyridopyrimidinone inhibitors of pi3k.alpha.
BRPI0617159B8 (en) * 2005-10-07 2021-05-25 Exelixis Inc pi3ka inhibitor pyridopyrimidinone compounds, compositions containing them, and preparation process
AU2007284562B2 (en) * 2006-08-16 2013-05-02 Exelixis, Inc. Using PI3K and MEK modulators in treatments of cancer
WO2008032162A1 (en) * 2006-09-15 2008-03-20 Pfizer Products Inc. Pyrido (2, 3-d) pyrimidin0ne compounds and their use as pi3 inhibitors

Also Published As

Publication number Publication date
MA31336B1 (en) 2010-04-01
EA200970936A1 (en) 2010-02-26
IL201209A0 (en) 2010-05-31
CA2683820A1 (en) 2008-10-23
US20100209340A1 (en) 2010-08-19
UA101315C2 (en) 2013-03-25
HK1139941A1 (en) 2010-09-30
AU2008239596B2 (en) 2013-08-15
MX2009010815A (en) 2009-10-29
US20130343988A1 (en) 2013-12-26
CO6241119A2 (en) 2011-01-20
JP2010523681A (en) 2010-07-15
DOP2009000242A (en) 2010-04-30
EP2142544B8 (en) 2013-07-03
ES2425068T3 (en) 2013-10-11
AU2008239596A1 (en) 2008-10-23
EP2142544B1 (en) 2013-05-22
TN2009000389A1 (en) 2010-12-31
NZ579945A (en) 2012-05-25
NI200900183A (en) 2010-10-05
CR11098A (en) 2010-01-27
CN101711249A (en) 2010-05-19
EP2142544A1 (en) 2010-01-13
WO2008127712A1 (en) 2008-10-23
EA018964B1 (en) 2013-12-30
KR20090130104A (en) 2009-12-17
SV2009003389A (en) 2010-04-27
MY150747A (en) 2014-02-28
ZA200906648B (en) 2010-04-28
BRPI0810175A2 (en) 2014-12-30

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